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Caffeine Metabolism
Fast or slow?
Eye Color Genetics
What your DNA says
Anger Intensity
Genetic temperament
Memory Formation
How you encode memories
Dream Vividness
Why dreams feel real
Endurance vs Power
Muscle fiber type
Sweet Tooth Gene
Sugar cravings explained
Cold Tolerance
Built for winter?
Caffeine Metabolism
Fast or slow?
Eye Color Genetics
What your DNA says
Anger Intensity
Genetic temperament
Memory Formation
How you encode memories
Dream Vividness
Why dreams feel real
Endurance vs Power
Muscle fiber type
Sweet Tooth Gene
Sugar cravings explained
Cold Tolerance
Built for winter?
Upload your raw genetic data and uncover insights about your health, medication responses, and unique traits. All processed privately in your browser. Nothing ever leaves your device.
🔒 30 traits free · 381 premium traits unlocked for $49
Health Risks
Cardiovascular, cancer, metabolic, neurological — with odds ratios and percentile rankings against population data.
Medication Check
See how your genes affect SSRIs, pain meds, statins, blood thinners, and more. Based on CPIC clinical guidelines.
Genetic Traits
Caffeine metabolism, sleep chronotype, pain sensitivity, muscle type, and hundreds more decoded from your DNA.
Example Findings from Real Reports
DPYD — 5-FU Toxicity Risk
Chemo drug sensitivity flagged
CYP2D6 — Poor SSRI Metabolizer
May need adjusted antidepressant dose
SLCO1B1 — Statin Myopathy Risk
Higher risk of muscle pain on statins
APOE ε2 — Alzheimer's Protection
40-50% reduced risk variant
See It In Action
Not Just Data. Personalized Insights
Every report includes actionable recommendations tailored to your unique genetic profile. See what's working for you, what to optimize, and exactly how to do it.
Cognitive Profile
Your brain's genetic blueprint
Learning Capacity
Room to optimize
Working Memory
Room to optimize
Processing Speed
Room to optimize
Cognitive Resilience
Room to optimize
Personalized Recommendation
Your BDNF variant is associated with enhanced response to aerobic exercise (30+ min, 4x/week), which research links to improved cognitive function.
Sleep & Circadian
Chronotype & sleep genetics
Night Owl
CLOCK gene: CC genotype
Sleep Depth
Deep Sleeper
Sleep Talking
Higher risk
Caffeine Sensitivity
Slow metabolizer
Your Optimal Schedule
Based on your genes: Sleep 12:30am–8:30am. Peak focus: 10am–1pm & 4pm–7pm.
Health Risks
52 conditions analyzed
These are just 3 of 27+ report tabs in your full analysis.
481 Genetic Traits
Decoded From Your DNA
From caffeine metabolism to dream vividness, sleep talking to pain sensitivity. Discover the quirks written into your genetic code. It's the most fun part of your report, and users can't stop sharing their results.
Free Tier
100
traits included
Premium
481
traits unlocked
🧬✨🔬"I spent an hour going through all my traits" . Every user ever
Caffeine Metabolism
Fast or slow?
Eye Color Genetics
What your DNA says
Anger Intensity
Genetic temperament
Memory Formation
How you encode memories
Dream Vividness
Why dreams feel real
Endurance vs Power
Muscle fiber type
Sweet Tooth Gene
Sugar cravings explained
Cold Tolerance
Built for winter?
Musical Ability
Perfect pitch potential
Sleep Talking
Nighttime chatter risk
Sense of Direction
Natural navigator?
Photic Sneeze Reflex
Sun makes you sneeze?
Caffeine Metabolism
Fast or slow?
Eye Color Genetics
What your DNA says
Anger Intensity
Genetic temperament
Memory Formation
How you encode memories
Dream Vividness
Why dreams feel real
Endurance vs Power
Muscle fiber type
Sweet Tooth Gene
Sugar cravings explained
Cold Tolerance
Built for winter?
Musical Ability
Perfect pitch potential
Sleep Talking
Nighttime chatter risk
Sense of Direction
Natural navigator?
Photic Sneeze Reflex
Sun makes you sneeze?
Lactose Tolerance
Dairy friend or foe?
Muscle Composition
Sprint or marathon?
Hair Curl Pattern
Straight, wavy, or curly
Alcohol Flush
The Asian glow gene
Cilantro Taste
Soapy or delicious?
Empathy Level
Oxytocin receptor type
ADHD Tendency
Attention & focus genes
Sleep Depth
Light or heavy sleeper?
Wisdom Teeth
Will they come in?
Asparagus Smell
Can you detect it?
Animal Bonding
Pet person genetics
Pain Sensitivity
High or low threshold?
Lactose Tolerance
Dairy friend or foe?
Muscle Composition
Sprint or marathon?
Hair Curl Pattern
Straight, wavy, or curly
Alcohol Flush
The Asian glow gene
Cilantro Taste
Soapy or delicious?
Empathy Level
Oxytocin receptor type
ADHD Tendency
Attention & focus genes
Sleep Depth
Light or heavy sleeper?
Wisdom Teeth
Will they come in?
Asparagus Smell
Can you detect it?
Animal Bonding
Pet person genetics
Pain Sensitivity
High or low threshold?
Freckling Tendency
Sun-kissed genes
Baldness Risk
Hair loss prediction
Bitter Taste Perception
Supertaster?
Stress Resilience
Warrior or worrier?
Night Vision
See in the dark?
Ticklishness
Somatosensory wiring
Twin Probability
Fraternal twin genes
Breath Hold Ability
Hypoxia tolerance
Static Shock Prone
Always getting zapped?
Longevity Markers
Built to last?
Placebo Response
Mind over medicine?
Decision Speed
Fast or deliberate?
Freckling Tendency
Sun-kissed genes
Baldness Risk
Hair loss prediction
Bitter Taste Perception
Supertaster?
Stress Resilience
Warrior or worrier?
Night Vision
See in the dark?
Ticklishness
Somatosensory wiring
Twin Probability
Fraternal twin genes
Breath Hold Ability
Hypoxia tolerance
Static Shock Prone
Always getting zapped?
Longevity Markers
Built to last?
Placebo Response
Mind over medicine?
Decision Speed
Fast or deliberate?
From Our Blog
Learn More About Your DNA
Explore our most popular articles on genetics, health insights, and how to get more from your DNA test results.
Caffeine Metabolism: Why Some People Can't Sleep After Coffee
Discover how your CYP1A2 gene affects caffeine breakdown and whether you're a fast or slow metabolizer.
23andMe Shutting Down? How to Save Your DNA Data
Step-by-step guide to download your raw DNA data before it's too late, and what to do with it.
APOE4 & Alzheimer's: What Your DNA Actually Means
Understanding your APOE4 status, risk factors, and lifestyle interventions that actually matter.
Check Drug Interactions With Your DNA
How pharmacogenomics helps predict which medications work best for your unique genetic profile.
Why GenomeInsight
What Makes GenomeInsight Different
100% Private
Your DNA file is processed entirely in your browser. Nothing is uploaded, stored, or shared. Ever. We literally can't see your data.
One Payment, Not a Subscription
Pay $49 once and own your analysis forever. No monthly fees, no annual renewals, no surprise charges. SelfDecode charges $99/year. Nebula charges $149/year.
27 Reports, Not a Summary
Most DNA services give you a pie chart. We give you 27 interactive tabs: health risks with odds ratios, drug interactions, cognitive profile, sleep genetics, longevity score, and 481 decoded traits.
Our Sources
Powered by Real Research
Health risk and pharmacogenomics analysis drawn from leading clinical and genomics databases
ClinVar
NCBI clinical variant database
GWAS Catalog
Genome-wide association studies
PharmGKB
Pharmacogenomics knowledge base
CPIC
Clinical Pharmacogenetics Implementation Consortium
Pricing
Simple, Transparent Pricing
Comparable services charge $99–$199/year. We charge once.
Free
Start with 30 traits instantly
- 30 genetic traits analyzed
- Basic ancestry composition
- Raw data browser
Premium
Unlock everything — 481 traits
- Everything in Free
- All 481 genetic traits
- Health risk analysis (52 conditions)
- Pharmacogenomics (14 genes, 50+ drugs)
- Cognitive & mental health profile
SelfDecode: $99/year · Nebula: $149/year · GenomeInsight: $100 $49 once
Limited time offer — No subscription required
FAQ
Frequently Asked Questions
Everything you need to know about GenomeInsight.
Absolutely. GenomeInsight processes everything directly in your browser using client-side JavaScript. Your raw genetic data file is never uploaded to any server. No network requests are made with your DNA data. It stays on your device, period.
You can download your raw data from services like 23andMe, AncestryDNA, or MyHeritage. Each provider has a "Download Raw Data" option in their account settings. The file is typically a .txt or .csv file containing your genotyped SNP data.
Our analysis is based on peer-reviewed GWAS (Genome-Wide Association Studies), ClinVar pathogenicity classifications, CPIC pharmacogenomics guidelines, and established population genetics research. However, consumer genotyping covers only a fraction of your genome. Results are informational — not diagnostic.
No. GenomeInsight is strictly an educational and informational tool. It is NOT a medical device, diagnostic test, or clinical service. Genetic risk factors are just one piece of the puzzle — lifestyle, environment, and family history all matter. Always consult a qualified healthcare provider before making medical decisions.
We support raw data exports from 23andMe (.txt), AncestryDNA (.txt), MyHeritage (.csv), and standard VCF files (.vcf). The parser auto-detects the format and extracts SNP data accordingly.
No account is needed for the free tier. Simply visit the site, upload your file, and explore your traits and basic ancestry instantly. For health risks, pharmacogenomics, and premium reports, you'll create an account after purchasing.
Pharmacogenomics (PGx) studies how your genes affect your response to medications. For example, variants in CYP2D6 can make you a poor or ultra-rapid metabolizer of certain drugs like codeine or tamoxifen. Our report analyzes 14 pharmacogenes covering 50+ medications based on CPIC clinical guidelines.
Your genetic data is fixed, but our analysis database grows. As new research is published and we add more variants, re-uploading your file will give you an updated, more comprehensive report. Premium users get lifetime access to all future updates.